EP1764112A2 - Copolymères linéaires de cyclodextrine - Google Patents

Copolymères linéaires de cyclodextrine Download PDF

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Publication number
EP1764112A2
EP1764112A2 EP06024721A EP06024721A EP1764112A2 EP 1764112 A2 EP1764112 A2 EP 1764112A2 EP 06024721 A EP06024721 A EP 06024721A EP 06024721 A EP06024721 A EP 06024721A EP 1764112 A2 EP1764112 A2 EP 1764112A2
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Prior art keywords
cyclodextrin
copolymer
linear
deoxy
moieties
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German (de)
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EP1764112B1 (fr
EP1764112A3 (fr
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Mark E. Davis
Hector Gonzales
Susie Hwang (Sue Jean)
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California Institute of Technology
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California Institute of Technology
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
    • C08B37/0012—Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S977/00—Nanotechnology
    • Y10S977/70—Nanostructure
    • Y10S977/788—Of specified organic or carbon-based composition
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S977/00—Nanotechnology
    • Y10S977/902—Specified use of nanostructure
    • Y10S977/904—Specified use of nanostructure for medical, immunological, body treatment, or diagnosis
    • Y10S977/906—Drug delivery

Definitions

  • the invention relates to linear cyclodextrin copolymers and linear oxidized cyclodextrin copolymers. These copolymers, respectively, contain a cyclodextrin moiety, unoxidized or oxidized, as a monomer unit integrated into the copolymer backbone.
  • the invention also relates methods of preparing linear cyclodextrin copolymers and linear oxidized cyclodextrin copolymers. Such cyclodextrin copolymers may be used as a delivery vehicle of various therapeutic agents.
  • Cyclodextrins are cyclic polysaccharides containing naturally occurring D(+)-glucopyranose units in an ⁇ -(1,4) linkage.
  • the most common cyclodextrins are alpha ( ⁇ )-cyclodextrins, beta ( ⁇ )-cyclodextrins and gamma ( ⁇ )-cyclodextrins which contain, respectively six, seven or eight glucopyranose units.
  • the cyclic nature of a cyclodextrin forms a torus or donut-like shape having an inner apolar or hydrophobic cavity, the secondary hydroxyl groups situated on one side of the cyclodextrin torus and the primary hydroxyl groups situated on the other.
  • a cyclodextrin is often represented schematically as follows: The side on which the secondary hydroxyl groups are located has a wider diameter than the side on which the primary hydroxyl groups are located.
  • the hydrophobic nature of the cyclodextrin inner cavity allows for the inclusion of a variety of compounds.
  • Cyclodextrins have been used as a delivery vehicle of various therapeutic compounds by forming inclusion complexes with various drugs that can fit into the hydrophobic cavity of the cyclodextrin or by forming non-covalent association complexes with other biologically active molecules such as oligonucleotides and derivatives thereof.
  • U.S. Patent 4,727,064 describes pharmaceutical preparations consisting of a drug with substantially low water solubility and an amorphous, water-soluble cyclodextrin-based mixture. The drug forms an inclusion complex with the cyclodextrins of the mixture.
  • U.S. Patent 5,691,316 a cyclodextrin cellular delivery system for oligonucleotides is described.
  • an oligonucleotide is noncovalently complexed with a cyclodextrin or, alternatively, the oligonucleotide may be covalently bound to adamantine which in turn is non-covalently associated with a cyclodextrin.
  • cyclodextrin containing polymers and methods of their preparation are also known in the art. ( Comprehensive Supramolecular Chemistry, Volume 3, J.L. Atwood et al., eds., Pergamon Press (1996 )).
  • a process for producing a polymer containing immobilized cyclodextrin is described in U.S. Patent 5,608,015 .
  • a cyclodextrin derivative is reacted with either an acid halide monomer of an ⁇ , ⁇ -unsaturated acid or derivative thereof or with an ⁇ , ⁇ -unsaturated acid or derivative thereof having a terminal isocyanate group or a derivative thereof.
  • the cyclodextrin derivative is obtained by reacting cyclodextrin with such compounds as carbonyl halides and acid anhydrides.
  • the resulting polymer contains cyclodextrin units as side chains off a linear polymer main chain.
  • U.S. Patent 5,276,088 describes a method of synthesizing cyclodextrin polymers by either reacting polyvinyl alcohol or cellulose or derivatives thereof with cyclodextrin derivatives or by copolymerization of a cyclodextrin derivative with vinyl acetate or methyl methacrylate. Again, the resulting cyclodextrin polymer contains a cyclodextrin moiety as a pendant moiety off the main chain of the polymer.
  • a biodegradable medicinal polymer assembly with supermolecular structure is described in WO 96/09073 A1 .
  • the assembly comprises a number of drug-carrying cyclic compounds prepared by binding a drug to an ⁇ , ⁇ , or ⁇ -cyclodextrin and then stringing the drug/cyclodextrin compounds along a linear polymer with the biodegradable moieties bound to both ends of the polymer.
  • Such an assembly is reportably capable of releasing a drug in response to a specific biodegradation occurring in a disease.
  • These assemblies are commonly referred to as "necklace-type" cyclodextrin polymers.
  • Such a linear cyclodextrin copolymer has a repeating unit of formula Ia, Ib, or a combination thereof:
  • the invention also provides methods of preparing a linear cyclodextrin copolymer.
  • One method copolymerizes a cyclodextrin monomer precursor disubstituted with the same or different leaving group and a comonomer A precursor capable of displacing the leaving group.
  • Another such method involves iodinating a cyclodextrin monomer precursor to form a diiodinated cyclodextrin monomer precursor and then copolymerizing the diiodinated cyclodextrin monomer precursor with a comonomer A precursor to produce the linear cyclodextrin copolymer.
  • Another method involves iodinating a cyclodextrin monomer precursor to form a diiodinated cyclodextrin monomer precursor, aminating the diiodinated cyclodextrin monomer precursor to form a diaminated cyclodextrin monomer precursor and then copolymerizing the diaminated cyclodextrin monomer precursor with a comonomer A precursor to produce the linear cyclodextrin copolymer.
  • Yet another method involves the reduction of a linear oxidized cyclodextrin copolymer to the linear cyclodextrin copolymer.
  • the invention further provides a linear oxidized cyclodextrin copolymer.
  • a linear oxidized cyclodextrin copolymer is a linear cyclodextrin copolymer which contains at least one oxidized cyclodextrin moiety of formula VIa or VIb:
  • Each cyclodextrin moiety of a linear cyclodextrin copolymer of the invention may be oxidized so as to form a linear oxidized cyclodextrin copolymer having a repeating unit of formula VIa, VIb, or a combination thereof.
  • the invention also provides a method of preparing a linear oxidized cyclodextrin copolymer.
  • One method involves oxidizing a linear cyclodextrin copolymer such that at least one cyclodextrin monomer is oxidized.
  • Other methods involve copolymerizing an oxidized cyclodextrin monomer precursor with a comonomer A precursor.
  • the invention still further provides a linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer grafted onto a substrate and a method of their preparation.
  • the invention also provides a linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer crosslinked to another polymer and a method of their preparation.
  • a method of preparing crosslinked cyclodextrin polymers involves reacting a linear or linear oxidized cyclodextrin copolymer with a polymer in the presence of a crosslinking agent.
  • the invention provides a linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer having at least one ligand bound to the cyclodextrin copolymer.
  • the ligand may be bound to either the cyclodextrin moiety or the comonomer A moiety of the copolymer.
  • the invention also provides a cyclodextrin composition containing at least one linear cyclodextrin copolymer of the invention and at least one linear oxidized cyclodextrin copolymer of the invention.
  • the invention also provides therapeutic compositions containing a therapeutic agent and a linear cyclodextrin copolymer and/or a linear oxidized cyclodextrin copolymer of the invention. A method of treatment by administering a therapeutically effective amount of a therapeutic composition of the invention is also described.
  • a linear cyclodextrin copolymer is a polymer containing cyclodextrin moieties as an integral part of its polymer backbone. Previously, cyclodextrin moieties were not a part of the main polymer chain but rather attached off a polymer backbone as pendant moieties.
  • a linear cyclodextrin copolymer has a repeating unit of formula Ia, Ib, or a combination thereof: In formula Ia and Ib, C is a substituted or unsubstituted cyclodextrin monomer and A is a comonomer bound, i.e.
  • cyclodextrin C covalently bound, to cyclodextrin C.
  • Polymerization of a cyclodextrin monomer C precursor with a comonomer A precursor results in a linear cyclodextrin copolymer of the invention.
  • the cyclodextin monomer C unit may be the same or different and, likewise, the comonomer A may be the same or different.
  • a cyclodextrin monomer precursor may be any cyclodextrin or derivative thereof known in the art.
  • a cyclodextrin is defined as a cyclic polysaccharide most commonly containing six to eight naturally occurring D(+)-glucopyranose units in an ⁇ -(1,4) linkage.
  • the cyclodextrin monomer precursor is a cyclodextrin having six, seven and eight glucose units, i.e., respectively, an alpha ( ⁇ )-cyclodextrin, a beta ( ⁇ )-cyclodextrin and a gamma (y)-cyclodextrin.
  • a cyclodextrin derivative may be any substituted cyclodextrin known in the art where the substituent does not interfere with copolymerization with comonomer A precursor as described below. According to the invention, a cyclodextrin derivative may be neutral, cationic or anionic.
  • substituents include, but are not limited to, hydroxyalkyl groups, such as, for example, hydroxypropyl, hydroxyethyl; ether groups, such as, for example, dihydroxypropyl ethers, methyl-hydroxyethyl ethers, ethyl-hydroxyethyl ethers, and ethyl-hydroxypropyl ethers; alkyl groups, such as, for example, methyl; saccharides, such as, for example, glucosyl and maltosyl; acid groups, such as, for example, carboxylic acids, phosphorous acids, phosphinous acids, phosphonic acids, phosphoric acids, thiophosphonic acids, thiophosphonic acid and sulfonic acids; imidazole groups; and sulfate groups.
  • hydroxyalkyl groups such as, for example, hydroxypropyl, hydroxyethyl
  • ether groups such as, for example, dihydroxypropyl ethers, methyl-hydroxy
  • a cyclodextrin monomer precursor may be further chemically modified (e.g. halogenated, aminated) to facilitate or affect copolymerization of the cyclodextrin monomer precursor with a comonomer A precursor, as described below.
  • Chemical modification of a cyclodextrin monomer precursor allows for polymerization at only two positions on each cyclodextrin moiety, i.e. the creation of a bifunctional cyclodextrin moiety.
  • the numbering scheme for the C1-C6 positions of each glucopyranose ring is as follows: In a preferred embodiment, polymerization occurs at two of any C2, C3 and C6 position, including combinations thereof, of the cyclodextrin moiety.
  • one cyclodextrin monomer precursor may be polymerized at two C6 positions while another cyclodextrin monomer precursor may be polymerized at a C2 and a C6 position of the cyclodextrin moiety.
  • the lettering scheme for the relative position of each glucopyranose ring in a cyclodextrin is as follows:
  • the cyclodextrin monomer C has the following general formula (II):
  • n and m represent integers which, along with the other two glucopyranose rings, define the total number of glucopyranose units in the cyclodextrin monomer.
  • Formula (II) represents a cyclodextrin monomer which is capable of being polymerized at two C6 positions on the cyclodextrin unit.
  • formula (III) one of D(+)-glucopyranose units of a cyclodextrin monomer has undergone ring opening to allow for polymerization at a C2 and a C3 position of the cyclodextrin unit.
  • Cyclodextrin monomers of formula (III) are commercially available from Carbomer of West borough, MA.
  • Examples of cyclodextrin monomers of formula (III) include, but are not limited to, 2 A ,3 A -deoxy-2 A ,3 A -dihydro- ⁇ -cyclodextrin, 2 A ,3 A -deoxy-2 A ,3 A -dihydro- ⁇ -cyclodextrin, 2 A ,3 A -deoxy-2 A ,3 A -dihydro- ⁇ -cyclodextrin, commonly referred to as, respectively, 2,3-deoxy- ⁇ -cyclodextrin, 2,3-deoxy- ⁇ -cyclodextrin, and 2,3-deoxy- ⁇ -cyclodextrin.
  • a comonomer A precursor may be any straight chain or branched, symmetric or asymmetric compound which upon reaction with a cyclodextrin monomer precursor, as described above, links two cyclodextrin monomers together.
  • a comonomer A precursor is a compound containing at least two functional groups through which reaction and thus linkage of the cyclodextrin monomers can be achieved.
  • Examples of possible functional groups, which may be the same or different, terminal or internal, of each comonomer A precursor include, but are not limited to, amino, acid, ester, imidazole, and acyl halide groups and derivatives thereof.
  • the two functional groups are the same and terminal.
  • two cyclodextrin monomers may be linked together by joining the primary hydroxyl side of one cyclodextrin monomer with the primary hydroxyl side of another cyclodextrin monomer, by joining the secondary hydroxyl side of one cyclodextrin monomer with the secondary hydroxyl side of another cyclodextrin monomer, or by joining the primary hydroxyl side of one cyclodextrin monomer with the secondary hydroxyl side of another cyclodextrin monomer. Accordingly, combinations of such linkages may exist in the final copolymer.
  • Both the comonomer A precursor and the comonomer A of the final copolymer may be neutral, cationic (e.g. by containing protonated groups such as, for example, quaternary ammonium groups) or anionic ( e.g. by containing deprotonated groups, such as, for example, sulfate, phosphate or carboxylate anionic groups).
  • the charge of comonomer A of the copolymer may be adjusted by adjusting pH conditions.
  • Suitable comonomer A precursors include, but are not limited to, cystamine, 1,6-diaminohexane, diimidazole, dithioimidazole, spermine, dithiospermine, dihistidine, dithiohistidine, succinimide (e.g . dithiobis(succinimidyl propionate) (DSP) and disuccinimidyl suberate (DSS)) and imidates (e.g. dimethyl 3,3'-dithiobispropionimidate (DTBP)).
  • cystamine 1,6-diaminohexane
  • diimidazole dithioimidazole
  • spermine dithiospermine
  • dihistidine dithiohistidine
  • succinimide e.g . dithiobis(succinimidyl propionate) (DSP) and disuccinimidyl suberate (DSS)
  • imidates e.g.
  • Copolymerization of a comonomer A precursor with a cyclodextrin monomer precursor leads to the formation of a linear cyclodextrin copolymer of the invention containing comonomer A linkages of the following general formulae: -HNC(O)(CH 2 ) x C(O)NH-, -HNC(O)(CH 2 ) x SS(CH 2 ) x C(O)NH-, - + H 2 N(CH 2 ) x SS(CH 2 ) x NH 2 + -, -HNC(O)(CH 2 CH 2 O) x CH 2 CH 2 C(O)NH-, -HNNHC(O)(CH 2 CH 2 O) x CH 2 CH 2 C(O)NHNH-, - + H 2 NCH 2 (CH 2 CH 2 O) x CH 2 CH 2 CH 2 NH 2 + -, -HNC(O)(CH 2 CH 2 O) x CH 2 CH 2
  • comonomer A is biodegradable or acid-labile.
  • the comonomer A precursor and hence the comonomer A may be selectively chosen in order to achieve a desired application. For example, to deliver small molecular therapeutic agents, a charged polymer may not be necessary and the comonomer A may be a polyethylene glycol group.
  • a linear cyclodextrin copolymer of the invention may be modified with at least one ligand attached to the cyclodextrin copolymer.
  • the ligand may be attached to the cyclodextrin copolymer through the cyclodextrin monomer C or comonomer A.
  • the ligand is attached to at least one cyclodextrin moiety of the linear cyclodextrin copolymer.
  • the ligand allows a linear cyclodextrin copolymer to target and bind to a cell.
  • the additional ligand or ligands may be bound to the same or different cyclodextrin moiety or the same or different comonomer A of the copolymer.
  • suitable ligands include, but are not limited to, vitamins (e.g, folic acid), proteins (e.g. transferrin, and monoclonal antibodies) and polysaccharides. The ligand will vary depending upon the type of delivery desired.
  • receptor-mediated delivery may by achieved by, but not limited to, the use of a folic acid ligand while antisense oligo delivery may be achieved by, but not limited to, use of a transferrin ligand.
  • the ligand may be attached to a copolymer of the invention by means known in the art.
  • a linear cyclodextrin copolymer of the invention may be prepared by copolymerizing a cyclodextrin monomer precursor disubstituted with an appropriate leaving group with a comonomer A precursor capable of displacing the leaving groups.
  • the leaving group which may be the same or different, may be any leaving group known in the art which may be displaced upon copolymerization with a comonomer A precursor.
  • a linear cyclodextrin copolymer may be prepared by iodinating a cyclodextrin monomer precursor to form a diiodinated cyclodextrin monomer precursor and copolymerizing the diiodinated cyclodextrin monomer precursor with a comonomer A precursor to form a linear cyclodextrin copolymer having a repeating unit of formula Ia, Ib, or a combination thereof, each as described above.
  • a method of preparing a linear cyclodextrin of the invention iodinates a cyclodextrin monomer precursor as described above to form a diiodinated cyclodextrin monomer precursor of formula IVa, IVb, IVc or a mixture thereof:
  • the diiodinated cyclodextrin may be prepared by any means known in the art. ( Tabushi et al. J. Am. Chem. 106, 5267-5270 (1984) ; Tabushi et al. J. Am. Chem. 106, 4580-4584 (1984) ).
  • ⁇ -cyclodextrin may be reacted with biphenyl-4,4'-disulfonyl chloride in the presence of anhydrous pyridine to form a biphenyl-4,4'-disulfonyl chloride capped ⁇ -cyclodextrin which may then be reacted with potassium iodide to produce diiodo- ⁇ -cyclodextrin.
  • the cyclodextrin monomer precursor is iodinated at only two positions.
  • a linear cyclodextrin polymer having a repeating unit of formula Ia, Ib, or a combination thereof, also as described above may be prepared. If appropriate, the iodine or iodo groups may be replaced with other known leaving groups.
  • the iodo groups or other appropriate leaving group may be displaced with a group that permits reaction with a comonomer A precursor, as described above.
  • a diiodinated cyclodextrin monomer precursor of formula IVa, IVb, IVc or a mixture thereof may be aminated to form a diaminated cyclodextrin monomer precursor of formula Va, Vb, Vc or a mixture thereof:
  • the diaminated cyclodextrin monomer precursor may be prepared by any means known in the art. ( Tabushi et al. Tetrahedron Lett. 18:1527-1530 (1977 ); Mungall et al., J. Org. Chem.
  • a diiodo- ⁇ -cyclodextrin may be reacted with sodium azide and then reduced to form a diamino- ⁇ -cyclodextrin.
  • the cyclodextrin monomer precursor is aminated at only two positions.
  • the diaminated cyclodextrin monomer precursor may then be copolymerized with a comonomer A precursor, as described above, to produce a linear cyclodextrin copolymer having a repeating unit of formula Ia, Ib, or a combination thereof, also as described above.
  • amino functionality of a diaminated cyclodextrin monomer precursor need not be directly attached to the cyclodextrin moiety.
  • the amino functionality may be introduced by displacement of the iodo or other appropriate leaving groups of a cyclodextrin monomer precursor with amino group containing moieties such as, for example, -SCH 2 CH 2 NH 2 , to form a diaminated cyclodextrin monomer precursor of formula Vd, Ve, Vf or a mixture thereof:
  • a linear cyclodextrin copolymer of the invention may also be prepared by reducing a linear oxidized cyclodextrin copolymer of the invention as described below. This method may be performed as long as the comonomer A does not contain a reducible moiety or group such as, for example, a disulfide linkage.
  • a linear cyclodextrin copolymer of the invention may be oxidized so as to introduce at least one oxidized cyclodextrin monomer into the copolymer such that the oxidized cyclodextrin monomer is an integral part of the polymer backbone.
  • a linear cyclodextrin copolymer which contains at least one oxidized cyclodextrin monomer is defined as a linear oxidized cyclodextrin copolymer.
  • the cyclodextrin monomer may be oxidized on either the secondary or primary hydroxyl side of the cyclodextrin moiety.
  • a linear oxidized cyclodextrin copolymer with oxidized secondary hydroxyl groups has, for example, at least one unit of formula VIa or VIb: In formulae VIa and VIb, C is a substituted or unsubstituted oxidized cyclodextrin monomer and A is a comonomer bound, i. e.
  • a linear oxidized cyclodextrin copolymer may be prepared by oxidation of a linear cyclodextrin copolymer as discussed above. Oxidation of a linear cyclodextrin copolymer of the invention may be accomplished by oxidation techniques known in the art. ( Hisamatsu et al., Starch 44:188-191 (1992 )). Preferably, an oxidant such as, for example, sodium periodate is used. It would be understood by one of ordinary skill in the art that under standard oxidation conditions that the degree of oxidation may vary or be varied per copolymer.
  • a linear oxidized copolymer of the invention may contain one oxidized cyclodextrin monomer.
  • substantially all to all cyclodextrin monomers of the copolymer would be oxidized.
  • Another method of preparing a linear oxidized cyclodextrin copolymer of the invention involves the oxidation of a diiodinated or diaminated cyclodextrin monomer precursor, as described above, to form an oxidized diiodinated or diaminated cyclodextrin monomer precursor and copolymerization of the oxidized diiodinated or diaminated cyclodextrin monomer precursor with a comonomer A precursor.
  • an oxidized diiodinated cyclodextrin monomer precursor of formula VIIa, VIIb, VIIc, or a mixture thereof may be prepared by oxidation of a diiodinated cyclodextrin monomer precursor of formulae IVa, IVb, IVc, or a mixture thereof, as described above.
  • an oxidized diaminated cyclodextrin monomer precursor of formula VIIIa, VIIIb, VIIIc or a mixture thereof may be prepared by amination of an oxidized diiodinated cyclodextrin monomer precursor of formulae VIIa, VIIb, VIIc, or a mixture thereof, as described above.
  • an oxidized diaminated cyclodextrin monomer precursor of formula IXa, IXb, IXc or a mixture thereof may be prepared by displacement of the iodo or other appropriate leaving groups of an oxidized cyclodextrin monomer precursor disubstituted with an iodo or other appropriate leaving group with the amino group containing moiety -SCH 2 CH 2 NH 2 .
  • an oxidized diiodinated or diaminated cyclodextrin monomer precursor may be prepared by oxidizing a cyclodextrin monomer precursor to form an oxidized cyclodextrin monomer precursor and then diiodinating and/or diaminating the oxidized cyclodextrin monomer, as described above.
  • the cyclodextrin moiety may be modified with other leaving groups other than iodo groups and other amino group containing functionalities.
  • the oxidized diiodinated or diaminated cyclodextrin monomer precursor may then be copolymerized with a comonomer A precursor, as described above, to form a linear oxidized cyclodextrin copolymer of the invention.
  • a linear oxidized cyclodextrin copolymer may also be further modified by attachment of at least one ligand to the copolymer.
  • the ligand is as described above.
  • a linear cyclodextrin copolymer or a linear oxidized cyclodextrin copolymer terminates with at least one comonomer A precursor or hydrolyzed product of the comonomer A precursor, each as described above.
  • at least one free functional group exists per linear cyclodextrin copolymer or per linear oxidized cyclodextrin copolymer.
  • the functional group may be an acid group or a functional group that may be hydrolyzed to an acid group.
  • the functional group may be further chemically modified as desired to enhance the properties of the cyclodextrin copolymer, such as, for example, colloidal stability, and transfection efficiency.
  • the functional group may be modified by reaction with PEG to form a PEG terminated cyclodextrin copolymer to enhance colloidal stability or with histidine to form an imidazolyl terminated cyclodextrin copolymer to enhance intracellular and transfection efficiency.
  • the modified functional group may be used to extend a polymer chain by linking a linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer, as described herein, to the same or different cyclodextrin copolymer or to a non-cyclodextrin polymer.
  • the polymer to be added on is the same or different linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer which may also terminated with at least one comonomer A precursor for further modification, each as described herein.
  • At least two of the same or different linear cyclodextrin copolymers or linear oxidized cyclodextrin copolymers containing a terminal functional group or a terminal modified functional group, as described above, may be reacted and linked together through the functional or modified functional group.
  • a degradable moiety such as, for example, a disulfide linkage is formed.
  • modification of the terminal functional group with cysteine may be used to produce a linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer having at least one free thiol group.
  • the functional or modified functional groups may be selected to offer linkages exhibiting different rates of degradation (e.g . via enzymatic degradation) and thereby provide, if desired, a time release system for a therapeutic agent.
  • the resulting polymer may be crosslinked, as described herein.
  • a therapeutic agent, as described herein, may be added prior to or post crosslinking of the polymer.
  • a ligand, as described herein, may also be bound through the modified functional group.
  • a linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer may be attached to or grafted onto a substrate.
  • the substrate may be any substrate as recognized by those of ordinary skill in the art.
  • a linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer may be crosslinked to a polymer to form, respectively, a crosslinked cyclodextrin copolymer or a crosslinked oxidized cyclodextrin copolymer.
  • the polymer may be any polymer capable of crosslinking with a linear or linear oxidized cyclodextrin copolymer of the invention (e.g . polyethylene glycol (PEG) polymer, polyethylene polymer).
  • the polymer may also be the same or different linear cyclodextrin copolymer or linear oxidized cyclodextrin copolymer.
  • a linear cyclodextrin copolymer may be crosslinked to any polymer including, but not limited to, itself, another linear cyclodextrin copolymer, and a linear oxidized cyclodextrin copolymer.
  • a crosslinked linear cyclodextrin copolymer of the invention may be prepared by reacting a linear cyclodextrin copolymer with a polymer in the presence of a crosslinking agent.
  • a crosslinked linear oxidized cyclodextrin copolymer of the invention may be prepared by reacting a linear oxidized cyclodextrin copolymer with a polymer in the presence of an appropriate crosslinking agent.
  • the crosslinking agent may be any crosslinking agent known in the art. Examples of crosslinking agents include dihydrazides and disulfides.
  • the crosslinking agent is a labile group such that a crosslinked copolymer may be uncrosslinked if desired.
  • a linear cyclodextrin copolymer and a linear oxidized cyclodextrin copolymer of the invention may be characterized by any means known in the art. Such characterization methods or techniques include, but are not limited to, gel permeation chromatography (GPC), matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF Mass spec), 1 H and 13 C NMR, light scattering and titration.
  • GPC gel permeation chromatography
  • MALDI-TOF Mass spec matrix assisted laser desorption ionization-time of flight mass spectrometry
  • 1 H and 13 C NMR 1 H and 13 C NMR
  • the invention also provides a cyclodextrin composition containing at least one linear cyclodextrin copolymer and at least one linear oxidized cyclodextrin copolymer of the invention as described above. Accordingly, either or both of the linear cyclodextrin copolymer and linear oxidized cyclodextrin copolymer may be crosslinked to another polymer and/or bound to a ligand as described above.
  • Therapeutic compositions according to the invention contain a therapeutic agent and a linear cyclodextrin copolymer or a linear oxidized cyclodextrin copolymer, including crosslinked copolymers, of the invention.
  • the therapeutic agent may be any synthetic or naturally occurring biologically active therapeutic agent including those known in the art.
  • suitable therapeutic agents include, but are not limited to, antibiotics, steroids, polynucleotides (e.g. genomic DNA, cDNA, mRNA and antisense oligonucleotides), plasmids, peptides, peptide fragments, small molecules (e.g . doxorubicin) and other biologically active macromolecules such as, for example, proteins and enzymes.
  • a therapeutic composition of the invention may be prepared by means known in the art.
  • a copolymer of the invention is mixed with a therapeutic agent, as described above, and allowed to self-assemble.
  • the therapeutic agent and a linear cyclodextrin copolymer or a linear oxidized cyclodextrin copolymer of the invention associate with one another such that the copolymer acts as a delivery vehicle for the therapeutic agent.
  • the therapeutic agent and cyclodextrin copolymer may associate by means recognized by those of skill in the art such as, for example, electrostatic interaction and hydrophobic interaction.
  • the degree of association may be determined by techniques known in the art including, for example, fluorescence studies, DNA mobility studies, light scattering, electron microscopy, and will vary depending upon the therapeutic agent.
  • a therapeutic composition of the invention containing a copolymer of the invention and DNA may be used to aid in transfection, i.e. the uptake of DNA into an animal ( e.g . human) cell. ( Boussif, O. Proceedings of the National Academy of Sciences, 92:7297-7301 (1995 ); Zanta et al. Bioconjugate Chemistry, 8:839-844 (1997 )).
  • a therapeutic composition of the invention may be, for example, a solid, liquid, suspension, or emulsion.
  • a therapeutic composition of the invention is in a form that can be injected intravenously.
  • Other modes of administration of a therapeutic composition of the invention include, depending on the state of the therapeutic composition, methods known in the art such as, but not limited to, oral administration, topical application, parenteral, intravenous, intranasal, intraocular, intracranial or intraperitoneal injection.
  • a therapeutic composition of the invention may be used in a variety of therapeutic methods (e.g . DNA vaccines, antibiotics, antiviral agents) for the treatment of inherited or acquired disorders such as, for example, cystic fibrosis, Gaucher's disease, muscular dystrophy, AIDS, cancers ( e.g ., multiple myeloma, leukemia, melanoma, and ovarian carcinoma), cardiovascular conditions ( e.g., progressive heart failure, restenosis, and hemophilia), and neurological conditions (e.g., brain trauma).
  • a method of treatment administers a therapeutically effective amount of a therapeutic composition of the invention.
  • a therapeutically effective amount as recognized by those of skill in the art, will be determined on a case by case basis. Factors to be considered include, but are not limited to, the disorder to be treated and the physical characteristics of the one suffering from the disorder.
  • Another embodiment of the invention is a composition containing at least one biologically active compound having agricultural utility and a linear cyclodextrin copolymer or a linear oxidized cyclodextrin copolymer of the invention.
  • the agriculturally biologically active compounds include those known in the art.
  • suitable agriculturally biologically active compounds include, but are not limited to, fungicides, herbicides, insecticides, and mildewcides.
  • the present invention is summarized by the following items:
  • ⁇ -cyclodextrin (Cerestar USA, Inc. of Hammond, IN) was dried in vacuo ( ⁇ 0.1 mTorr) at 120°C for 12 h before use.
  • Biphenyl-4,4'-disulfonyl chloride (Aldrich Chemical Company, Inc. of Milwaukee, WI) was recrystallized from chloroform/hexanes.
  • Potassium iodide was powdered with a mortar and pestle and dried in an oven at 200°C. All other reagents were obtained from commercial suppliers and were used as received without further purification. Polymer samples were analyzed on a Hitachi HPLC system equipped with an Anspec RI detector and a Progel-TSK G3000 PWXL column using water as eluant at a 1.0 mL min -1 flow rate.
  • a 40 mL centrifuge tube equipped with a magnetic stirbar, a Schlenk adapter and a septum was charged with 1.02 g (7.2 mmol) of 1, 3.54 g (21.3 mmol) of dry, powdered potassium iodide (Aldrich) and 15 mL of anhydrous N,N-dimethylformamide (DMF) (Aldrich).
  • the resulting suspension was stirred at 80°C under nitrogen for 2 h. After cooling to room temperature, the solids were separated by centrifugation and the supernatant was decanted. The solid precipitate was washed with a second portion of anhydrous DMF and the supernatants were combined and concentrated in vacuo.
  • a 20 mL scintillation vial was charged with a solution of 92.6 mg (7.65 x 10 -5 mol) of the bis(hydrogen carbonate) salt of 4 in 1 mL of water.
  • the pH of the solution was adjusted to 10 with 1 M NaOH before a solution of 30.9 mg (7.65 x 10 -5 mol) of dithiobis(succinimidyl propionate) (DSP, Pierce Chemical Co. of Rockford, IL) in 1 mL of chloroform was added.
  • the resulting biphasic mixture was agitated with a Vortex mixer for 0.5 h.
  • the aqueous layer was then decanted and extracted with 3 x 1 mL of fresh chloroform.
  • aqueous polymer solution was then subjected to gel permeation chromatography (GPC) on Toyopearl HW-40F resin using water as eluant. Fractions were analyzed by GPC and appropriate fractions were lyophilized to yield 85 mg (85%) as a colorless amorphous powder.
  • GPC gel permeation chromatography
  • a ⁇ -cyclodextrin-DSS copolymer, 6, was synthesized in a manner analogous to the DSP polymer, 5, except that disuccinimidyl suberate (DSS, Pierce Chemical Co. of Rockford, IL) was substituted for the DSP reagent. Compound 6 was obtained in 67% yield.
  • Example 10 Oxidation of ⁇ -cyclodextrin-DSS copolymer, 10 (Hisamatsu et al., Starch 44, 188-191 (1992))
  • the ⁇ -cyclodextrin-DSS copolymer 6 (92.8 mg, 7.3 x 10 -5 mol) was dissolved in 1.0 mL of water and cooled in an ice bath before 14.8 mg (7.3 x 10 -5 mol) of sodium periodate was added. The solution immediately turned bright yellow and was allowed to stir in the dark at 0°C for 14 h. The solution was then subjected to gel permeation chromatography (GPC) on Toyopearl HW-40 resin using water as eluant. Fractions were analyzed by GPC. Appropriate fractions were combined and lyophilized to dryness to yield 84.2 mg (91 %) of a light brown amorphous solid.
  • GPC gel permeation chromatography
  • Example 12 ⁇ -cyclodextrin-PEG 600 copolymer
  • a 8 mL vial was charged with a solution of 102.3 mg (8.80 x 10-5 mol) of 2 A ,3 A -diamino-2 A ,3 A -deoxy- ⁇ -cyclodextrin in 1 mL of water.
  • the pH of the solution was adjusted to 10 with 1 M NaOH before a solution of 36.4 mg (8.80 x 10- 5 mol) of dithiobis(succinimidyl propionate) (DSP, Pierce Chemical Co. of Rockford, IL) in 1 mL of chloroform was added.
  • the resulting biphasic mixture was agitated with a Vortex mixer for 0.5h.
  • the aqueous layer was then decanted and extracted with 3 x 1 mL of fresh chloroform.
  • the aqueous polymer solution was then subjected to gel permeation chromatography.
  • Example 14 6 A ,6 D -Bis-(2-aminoethylthio)-6 A. 6 D -deoxy- ⁇ -cyclodextrin, 14 (Tabushi, I: Shimokawa, K; Fugita, K. Tetrahedron Lett. 1977 , 1527-1530)
  • Example 15 ⁇ -cyclodextrin(cystamine)-DTBP copolymer
  • aqueous polymer solution was then subjected to gel permeation chromatography on Toyopearl HW-40F resin. Fractions were analyzed by GPC and appropriate fractions were lyophilized to dryness. This afforded 21.3 mg (100%) of 15 as a white powder.
  • FMOC-PEG 3400 -NHS Shearwater Polymers, Inc. of Huntsville, AL
  • 1 mL of anhydrous N,N-dimethylformamide (DMF) is added to 10 equivalents of hydrazide 2-chlorotrityl resin (Novabiochem USA of La Jolla, CA) swelled in DMF.
  • the mixture is stirred at 60°C until all the polymer is coupled to the resin, as determined by a GPC system equipped with a UV detector.
  • the resin-polymer is then transferred to a sintered glass column for all further reactions.
  • the unreacted hydrazide groups on the resins are capped with acetic anhydride and the acetic acid products are neutralized by diisopropylethylamine.
  • the FMOC protecting group is removed by two washes with 20% piperidine in DMF (1 mL total volume). The resin is then washed 10 times with 1 mL DMF and 5 times with 1 mL H 2 O.
  • Folic acid-linker is reacted with 6 equivalents of a cyclodextrin copolymer (oxidized as in Example 10) by mixing in 50 mmol borate (pH 8.5). The reaction mixture is analyzed and conjugation polymer confirmed by a GPC system with a UV detection at 285 nm.
  • FMOC protecting group was removed with 20% piperidine in DMF. The solvent was removed in vacuo and product redissolved in 1.3 mL of DMSO.
  • Folic acid-linker is reacted with 6 equivalents of a cyclodextrin copolymer (oxidized as in Example 10) by mixing in 50 mmol borate (pH 8.5). The reaction mixture is analyzed and conjugation polymer confirmed by a GPC system with a UV detection at 285 nm.
  • iron-free human transferrin (Sigma of St. Louis, MO) is dissolved in 30 mM sodium acetate buffer and cooled to 0°C. To this solution is added 20 mg of sodium periodate dissolved in 4 ⁇ L of 30 mM sodium acetate. The mixture is stirred at 0°C overnight. Next 1 g of AG501-X8 resin (Biorad) is added to remove salts before the solution is lyophilized.
  • FMOC-PEG 3400 -NHS Shearwater Polymers, Inc. of Huntsville, AL
  • azide 2-chlorotrityl resin Novabiochem USA of La Jolla, CA
  • the resin-polymer was then transferred to a sintered glass column for all further reactions.
  • the unreacted hydrazide groups on the resins were capped with acetic anhydride and the acetic acid products were neutralized by diisopropylethylamine.
  • the FMOC protecting group was removed by two washes with 20% piperidine in DMF (1 mL total volume). The resin was then washed 10 times with 1 mL DMF and 5 times with 1 mL H 2 O.
  • Transferrin linker is reacted with 6 equivalents of a cyclodextrin copolymer by reductive amination with sodium cyanoborohydride: first, the copolymer is added to transferrin linker dissolved in 0.05 M sodium carbonate and 0.1 M sodium citrate buffer. 5 M cyanoborohydride in 1N NaOH is added and the reaction is stirred for 2 hours at room temperature. Unreacted aldehyde sites are blocked by adding ethanolamine and reacting for 15 minuted at room temperature. The resulting conjugate is purified by dialysis.
  • Cyclodextrin-based copolymer (CD-polymer) is dissolved in water, buffer, or organic solvent at the appropriate concentration. The small molecule is dissolved in a solvent miscible with the solvent of the CD-polymer solution and is added to the CD-polymer solution. The mixture is then stirred for 1 ⁇ 2 hour and then allowed to come to equilibrium overnight.
  • Copolymer 15 or 16 (138 ⁇ M equivalent of CD monomer) was not toxic to KB or KB-VI (a multidrug resistant derivative of KB) cell lines in the absence of doxorubicin.
  • a ligand such a folate is covalently attached to the CD-polymer used for doxorubicin complexation.
  • Cell Line CD-polymer IC 50 ( ⁇ M of doxorubicin) KB none -0.1 KB-VI (multidrug resistant) none -10 KB-VI copolymer 15 or 16 (138 ⁇ M equivalent of CD monomer) -2-3
  • 1 ⁇ g of DNA at a concentration of 0.2 ⁇ g/ ⁇ L in distilled water was mixed with 10 ⁇ L of copolymer 15 at polymer amine: DNA phosphate charge ratios of 2.4, 6, 12, 24, 36, 60, and 120.
  • the solution was mixed manually by a micropipette and then gently mixed overnight on a lab rotator.
  • 1 ⁇ g/ ⁇ L of loading buffer (40% sucrose, 0.25% bromophenol blue, and 200 mM Tris-Acetate buffer containing 5mM EDTA ( Gao et al., Biochemistry 35:1027-1036 (1996 )) was added to each solution the following morning.
  • Each DNA/polymer sample was loaded on a 0.6% agarose electrophoresis gel containing 6 ⁇ g of EtBr/100 mL in 1 x TAE buffer (40mM Tris-acetate/1 mM EDTA) and 40V was applied to the gel for 1 hour.
  • the extent of DNA/polymer complexation was indicated by DNA retardation in the gel migration pattern.
  • the polymer (15) retarded DNA at charge ratios of 6 and above, indicating complexation under these conditions.
  • Copolymer 15 or copolymer 16 is oxidized as in Example 10. Oxidized copolymer 15 or 16 is then complexed with a DNA plasmid as in Examples 23 and 26. A crosslinking agent (for example, PEG 600 -Dihydrazide) is then added to encapsulate the DNA. Encapsulation success is determined by light scattering and visualized by electron microscopy.
  • a crosslinking agent for example, PEG 600 -Dihydrazide
  • Equal volumes of a CD-polymer and DNA plasmid solutions in water are mixed in appropriate polymer/plasmid charge ratios.
  • the pH of the mixture is adjusted to form a charged CD-polymer.
  • the mixture is then allowed to equilibrate and self-assemble at room temperature for 30 minutes.
  • a crosslinking agent for example, PEG 600 -Dihydrazide
  • a concentrated buffer solution is then added to render the pH and thus the CD-polymer neutral. Encapsulation success is determined by light scattering and visualized by electron microscopy.
  • BHK-21 cells were plated in 24 well plates at a cell density of 60,000 cells/well 24 hours before transfection. Plasmids encoding the luciferase gene were encapsulated by the CD-polymer as in Examples 23 or 25 such that the DNA/polymer complexes were assembled at polymer amine: DNA phosphate charge ratios of 6, 12, 24, 36, and 60 as described in DNA binding studies of Example 23. Media solution containing the DNA/polymer complexes was added to cultured cells and replaced with fresh media after 5 hours of incubation at 37°C. The cells were lysed 48 hours after transfection. Appropriate substrates for the luciferase light assay were added to the cell lysate.
  • Luciferase activity measured in terms of light units produced, was quantified by a luminometer. DNA/polymer complexes successfully transfected BHK-21 cells at a charge ratios of 6, 12, and 24. Cell lysate was also used to determine cell viability by the Lowry protein assay. ( Lowry et al., Journal of Biological Chemistry, Vol. 193, 265-275 (1951) ). Maximum toxicity was seen at a polymer amine: DNA phosphate charge ratios of 36 and 60 with 91 % cell survival.
  • BHK-21 cells were plated in 24 well plates at a cell density of 60,000 cells/well 24 hours before transfection. Plasmids encoding the luciferase gene were encapsulated by the CD-polymer as in Example 23 except copolymer 15 was replaced with copolymer 16 and that the DNA/polymer complexes successfully transfected BHK-21 cells at charge ratios of 10, 20, 30, and 40 with maximum transfection at polymer amine:DNA phosphate charge ratio of 20. Media solution containing the DNA/polymer complexes was added to cultured cells and replaced with fresh media after 24 hours of incubation at 37°C. The cells were lysed 48 hours after transfection.
  • luciferase light assay Appropriate substrates for the luciferase light assay were added to the cell lysate. Luciferase activity, measured in terms of light units produced, was quantified by a luminometer. The results are illustrated below. DNA/polymer complexes successfully transfected BHK-21 cells at a charge ratios of 6, 12, and 24. Cell lysate was also used to determine cell viability by the Lowry protein assay. ( Lowry et al., Journal of Biological Chemistry, Vol. 193, 265-275 (1951) ). The results are illustrated below. Maximum toxicity was seen at a polymer amine: DNA phosphate charge ratios of 40 and 50 with 33% cell survival.
  • Plasmids encoding the green fluorescent protein are encapsulated by the CD-polymer as in Examples 23 or 25.
  • Media solution containing the DNA/polymer complexes is added to cultured cells and replaced with fresh media after 5 hours of incubation at 37°C.
  • the cells are detached from the surface with trypsin, washed, and resuspended in Hanks Balanced Salt Solution with propidium iodide.
  • the cells are then analyzed by fluorescence activated cell sorting (FACS). Cell viability is determined by cell size and propidium iodide exclusion, and transfection success by GFP protein fluorescence.
  • FACS fluorescence activated cell sorting
  • Antisense oligos directed against the luciferase gene are encapsulated by the CD-polymer as described in Example 29.
  • Media solution containing the oligo/polymer complexes is added to HeLa X1/5 cells (HeLa cells that constitutively express the luciferase gene, donated by CLONTECH) and replaced with fresh media after 5 hours of incubation at 37°C.
  • Cells are lysed 48 hours after transfection and appropriate substrates for the luciferase assay are added to the lysates.
  • Luciferase activity measured in terms of light units produced, is quantified by a luminometer. Transfection success is determined by knockout of luciferase activity.
  • Example 31 Toxicity of ⁇ -cyclodextrin(cystamine)-DTBP copolymer, 15
  • copolymer 15 The acute toxicity of copolymer 15 was investigated using Swiss-Webster "white mice.” A total of 48 mice were used as described in the table below. Single intravenous (i.v.) or intraperitoneal (i.p.) injections of sterile saline solutions or of copolymer 15 were given to the mice. The animals were followed for five days after which they sacrificed and gross necropsy performed. No mortality and no toxicity was observed. Group No.
  • Plasmids encoding the luciferase gene were encapsulated by the CD-polymer as in Example 23 except copolymer 15 was replaced with copolymer 16.
  • the DNA/polymer complexes were used to successfully transfect BHK-21 or CHO-K1 cells, each plated in 24 well plates at a cell density of 60,000 cells/well 24 hours before transfection, at various charge ratios in 10% serum and serum-free conditions following the procedure outlined in Example 27. The cells were lysed 48 hours after transfection. Appropriate substrates for the luciferase light assay were added to the cell lysate.
  • Luciferase activity measured in terms of light units produced (i.e., relative light units (RLU)), was quantified by a luminometer. Cell lysate was also used to determine cell viability by the Lowry protein assay. ( Lowry et al., Journal of Biological Chemistry, Vol. 193, 265-275 (1951) ). Toxicity was measured by determining total cellular protein in the wells 48 hours after transfection. The transfection and cell survival results in 10% serum and serum free media are illustrated below.
  • RLU relative light units
  • Luciferase protein activity in BHK-21 cells transfected in serum-free conditions reached a stable maximum at 30+/- with ⁇ 5 x 10 7 RLUs.
  • the presence of 10% serum in the transfection media decreased luciferase activity at all charge ratios except 70+/-.
  • With CHO-K1 cells, increasing charge ratio also enhanced the transfection for all conditions tested. Additionally, transfection in serum decreased light units by an order of magnitude.
  • Copolymer 16 showed toxicity only to BHK-21 cells for transfections in the absence of serum. Toxicity was minimized with the presence of 10% serum during transfection. No noticeable toxicity was observed from transfections to CHO-K1 cells. The effect of copolymer 16/DNA charge ratio and serum conditions on transfection efficiency (• and ⁇ ) and cell survival (V and ⁇ ) in BHK-21 cells. Results from transfection in 10% serum and serum-free media are shown as, respectively, dotted and solid lines. Data are reported as the mean +/- S.D. of three samples. Toxicity data are presented as best fit lines. The effect of copolymer 16/DNA charge ratio and serum conditions on transfection efficiency (• and ⁇ ) and cell survival (V and ⁇ ) in CHO-K1 cells. Results from transfection in 10% serum and serum-free media are shown as, respectively, dotted and solid lines. Data are reported as the mean +/- S.D. of three samples. Toxicity data are presented as best fit lines.
  • Example 32 transfection efficiency and toxicity of various non-viral vectors with BHK-21 and CHO-K1 cells were studied and compared against those achieved with DNA/copolymer 16 complexes.
  • the BHK-21 and CHO-K1 cells were transfected at a range of charge ratios and starting cell densities for all vectors in serum-free media. The results are illustrated below and illustrate the optimum transfection conditions found for each vector.

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ES2403416T3 (es) 2013-05-17
CA2336390A1 (fr) 2000-01-13
EP1093469B1 (fr) 2007-05-02
CN1308639A (zh) 2001-08-15
HUP0105472A3 (en) 2003-03-28
US6509323B1 (en) 2003-01-21
EP1764112B1 (fr) 2013-02-13
MXPA01000206A (es) 2002-10-17
ES2285844T3 (es) 2007-11-16
CA2336390C (fr) 2011-02-22
AU763114B2 (en) 2003-07-10
BR9911754A (pt) 2001-11-06
PT1093469E (pt) 2007-07-16
AU763114C (en) 2004-05-27
EP1764112A3 (fr) 2007-05-23
KR20010086293A (ko) 2001-09-10
ATE361321T1 (de) 2007-05-15
JP2011006695A (ja) 2011-01-13
IL140552A0 (en) 2002-02-10
DK1093469T3 (da) 2007-09-17
HUP0105472A2 (hu) 2002-05-29
IL140552A (en) 2006-10-31
HU229473B1 (en) 2014-01-28
JP2002519482A (ja) 2002-07-02
EP1093469A1 (fr) 2001-04-25
WO2000001734A1 (fr) 2000-01-13
DE69935982T2 (de) 2008-01-10
JP4741729B2 (ja) 2011-08-10
CN100365024C (zh) 2008-01-30
BR9911754B1 (pt) 2010-07-13
DE69935982D1 (en) 2007-06-14
AU4830599A (en) 2000-01-24
DK1764112T3 (da) 2013-03-11
KR100851315B1 (ko) 2008-08-08
CY1106797T1 (el) 2012-05-23

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